Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 5 |
GO:0032991 | protein-containing complex | 1 | 6 |
GO:0043226 | organelle | 2 | 5 |
GO:0043228 | non-membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:1990904 | ribonucleoprotein complex | 2 | 6 |
GO:0000314 | organellar small ribosomal subunit | 5 | 1 |
GO:0005763 | mitochondrial small ribosomal subunit | 3 | 1 |
GO:0015935 | small ribosomal subunit | 4 | 1 |
GO:0044391 | ribosomal subunit | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 6 |
GO:0006518 | peptide metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009059 | macromolecule biosynthetic process | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 6 |
GO:0043043 | peptide biosynthetic process | 5 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043603 | amide metabolic process | 3 | 6 |
GO:0043604 | amide biosynthetic process | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 6 |
GO:0005198 | structural molecule activity | 1 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.212 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.595 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.447 |
CLV_PCSK_PC7_1 | 420 | 426 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.420 |
DEG_MDM2_SWIB_1 | 271 | 278 | PF02201 | 0.364 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.552 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.482 |
DOC_CYCLIN_RxL_1 | 408 | 416 | PF00134 | 0.439 |
DOC_MAPK_gen_1 | 227 | 234 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 385 | 395 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 388 | 397 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 265 | 272 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.484 |
DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.397 |
DOC_SPAK_OSR1_1 | 170 | 174 | PF12202 | 0.397 |
DOC_USP7_UBL2_3 | 227 | 231 | PF12436 | 0.381 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.388 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 332 | 341 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 420 | 428 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 55 | 61 | PF00244 | 0.540 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_2 | 390 | 396 | PF00533 | 0.431 |
LIG_CtBP_PxDLS_1 | 289 | 293 | PF00389 | 0.497 |
LIG_EH1_1 | 280 | 288 | PF00400 | 0.265 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.448 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.651 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.440 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.394 |
LIG_LIR_Apic_2 | 344 | 348 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 23 | 31 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 391 | 399 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.442 |
LIG_Pex14_1 | 156 | 160 | PF04695 | 0.381 |
LIG_Pex14_2 | 271 | 275 | PF04695 | 0.381 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.418 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.429 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.430 |
LIG_SH2_SRC | 211 | 214 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.607 |
LIG_SH3_1 | 80 | 86 | PF00018 | 0.421 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.451 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.433 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.422 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.421 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.425 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.553 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.540 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.427 |
LIG_UBA3_1 | 103 | 112 | PF00899 | 0.536 |
LIG_UBA3_1 | 193 | 199 | PF00899 | 0.438 |
LIG_UBA3_1 | 393 | 400 | PF00899 | 0.484 |
MOD_CDK_SPxxK_3 | 105 | 112 | PF00069 | 0.410 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.442 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.445 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.686 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.663 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.403 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.420 |
MOD_CMANNOS | 76 | 79 | PF00535 | 0.429 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.431 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.408 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.573 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.576 |
MOD_LATS_1 | 54 | 60 | PF00433 | 0.665 |
MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.472 |
MOD_N-GLC_1 | 23 | 28 | PF02516 | 0.683 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.479 |
MOD_N-GLC_2 | 325 | 327 | PF02516 | 0.418 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.516 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.448 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.546 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.393 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.479 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.391 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.444 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.420 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.529 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.551 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.534 |
MOD_PKA_1 | 388 | 394 | PF00069 | 0.434 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.416 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.694 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.284 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.530 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.540 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.485 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.415 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.445 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.434 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.409 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.374 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.475 |
MOD_SUMO_for_1 | 37 | 40 | PF00179 | 0.638 |
MOD_SUMO_for_1 | 370 | 373 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 351 | 357 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_2 | 381 | 387 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 134 | 139 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 347 | 351 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF7 | Leptomonas seymouri | 90% | 100% |
A0A0S4J4D7 | Bodo saltans | 62% | 100% |
A0A1X0NWF9 | Trypanosomatidae | 81% | 100% |
A0A3S7WVW4 | Leishmania donovani | 99% | 100% |
A0A422NCH8 | Trypanosoma rangeli | 80% | 100% |
A4HYR0 | Leishmania infantum | 98% | 100% |
C9ZI69 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 80% | 100% |
E9AIA8 | Leishmania braziliensis | 93% | 100% |
Q4QCY9 | Leishmania major | 98% | 100% |